WO2008016626A2 - Stent hélicoïdal - Google Patents
Stent hélicoïdal Download PDFInfo
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- WO2008016626A2 WO2008016626A2 PCT/US2007/017152 US2007017152W WO2008016626A2 WO 2008016626 A2 WO2008016626 A2 WO 2008016626A2 US 2007017152 W US2007017152 W US 2007017152W WO 2008016626 A2 WO2008016626 A2 WO 2008016626A2
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- Prior art keywords
- stent
- elements
- helical
- strut
- strut members
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/82—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/86—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
- A61F2/90—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure
- A61F2/91—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
- A61F2/915—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes with bands having a meander structure, adjacent bands being connected to each other
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/82—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/86—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
- A61F2/90—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure
- A61F2/91—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/82—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/86—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
- A61F2/88—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure the wire-like elements formed as helical or spiral coils
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/82—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2002/823—Stents, different from stent-grafts, adapted to cover an aneurysm
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/82—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/848—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents having means for fixation to the vessel wall, e.g. barbs
- A61F2002/8486—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents having means for fixation to the vessel wall, e.g. barbs provided on at least one of the ends
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/82—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/86—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
- A61F2/90—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure
- A61F2/91—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
- A61F2/915—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes with bands having a meander structure, adjacent bands being connected to each other
- A61F2002/91533—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes with bands having a meander structure, adjacent bands being connected to each other characterised by the phase between adjacent bands
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/82—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/86—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
- A61F2/90—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure
- A61F2/91—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
- A61F2/915—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes with bands having a meander structure, adjacent bands being connected to each other
- A61F2002/9155—Adjacent bands being connected to each other
- A61F2002/91558—Adjacent bands being connected to each other connected peak to peak
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2220/00—Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2220/0008—Fixation appliances for connecting prostheses to the body
- A61F2220/0016—Fixation appliances for connecting prostheses to the body with sharp anchoring protrusions, e.g. barbs, pins, spikes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2230/00—Geometry of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2230/0002—Two-dimensional shapes, e.g. cross-sections
- A61F2230/0028—Shapes in the form of latin or greek characters
- A61F2230/0054—V-shaped
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2250/00—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2250/0014—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof having different values of a given property or geometrical feature, e.g. mechanical property or material property, at different locations within the same prosthesis
- A61F2250/0039—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof having different values of a given property or geometrical feature, e.g. mechanical property or material property, at different locations within the same prosthesis differing in diameter
Definitions
- the invention relates to a stent-like structure which in one embodiment can be used for treating neurovascular or brain aneurysms.
- a stent is a tubular structure that in a radially compressed state (crimped state) may be inserted into a vessel in the body. Once located in the vessel, the stent may be expanded radially to a predefined size (expanded state).
- Stents are typically characterized as balloon expanding or self expanding.
- a balloon expanding stent requires a balloon, which is part of the delivery system, to expand the stent from the crimped state to an expanded state.
- a self expanding stent is designed, through choice of material, geometry, or manufacturing techniques, to expand from a crimped state to an expanded state once the stent is released into the intended vessel.
- a stent is commonly thought of as a device that opens a narrowed artery.
- a stent-like structure has similar characteristics to a stent, but may not open or support an artery. Unless otherwise indicated, as used hereafter, the term "stent" will be understood to encompass both a stent and stent-like structure.
- An aneurysm is a weakened area in a vessel that has expanded or bulged. Untreated aneurysms are susceptible to rupture. Stenting of an aneurysm could strengthen the weakened vessel by cutting off significant blood flow to the aneurysm. The reduced blood flow could result in thrombosis in the aneurysm and promote healing regardless of the aneurysm form or shape. Stents have been used to treat aneurysms. Conventional stent grafts have been used to treat Thoracic and Abdominal Aortic Aneurysms. Stent grafts have a metallic stent structure covered by graft material.
- Stents have also been used experimentally to repair neurovascular aneurysms which were first treated with platinum coils that have migrated over time into the parent vessel. See Pride, Jr. et al., Endovascular problem solving with intravascular stents, AJNR Am J Neuroradiol. 2000; 21 :532-540.
- One system, Boston Scientific's Neuroform Microdelivery Stent System is described for use with embolic coils.
- Conventional treatment includes aneurysm clipping, which requires a craniotomy, or aneurysm coiling, placing small platinum or polymer coils in the aneurysm to facilitate thrombosis.
- the above-described conventional methods for treatment of neurovascular aneurysms have certain drawbacks.
- Coiling is effective when the aneurysm has a well defined neck (transition from the bulging portion of the vessel to the nominal vessel diameter). If this neck transition is wide or long, coiling is not as effective as the coils tend to migrate and cause other complications, as described in Lownie et al., Endovascular therapy of a large vertebral artery aneurysm using stent and coils, Can J Neurol Sd 2000; 27:162-165 andWanke et al., Treatment of wide-necked intracranial aneurysms with a self-expanding stent system: initial clinical experience, AJNR Am J Neuroradiol. 2003; 24:1192-1199. Clipping is very invasive, risky and expensive.
- Coronary stents typically have an expandable "Z" strut scaffolding structure that allows efficient radial expansion and effective vessel dilation. This type of structure requiring a large open area is not expected to be effective for treating neurovascular aneurysms because the large open areas would not inhibit blood flow. In coronary stents, radial expansion is achieved by opening the scaffolding structure to produce a structure that is mostly open area. Coronary stents typically have 75% to 90% open area (10 to 25% vessel coverage).
- the percent of the vessel covered would need to be at least about 35%. It is desirable to provide a stent for treating neurovascular or brain aneurysms having the percent of the vessel covered of at least about 35%.
- the present invention relates to a stent providing a high percentage of vessel coverage, preferably at least about 50% of the portion of the vessel covered by the helical elements of the stent.
- the stent comprises helical elements interposed between strut members in which the helical elements are connected to the strut members by linking elements.
- the strut members provide radial structure of the stent and an anchoring mechanism.
- the portion of the stent having helical elements provides a high percentage of covered area for example, in an aneurysm area.
- the linking elements provide part of a mechanism that allows vessel coverage to be maintained as the stent is deployed from a crimped state to an expanded state.
- vessel coverage in the expanded state is primarily achieved by shortening the pitch (distance per turn) of the helical elements during radial expansion.
- the linking element between the strut members and helical elements is part of a mechanism allowing the helical elements to change its helix angle (the angle at which the helical elements progresses around the circumference and along the length of the stent) and thereby the pitch of the helical elements as the stent is expanded.
- Fig. IA is a plan view of a first embodiment of the stent of the present invention including helical elements interposed between strut members and connected to the strut members by flexible linking elements.
- Fig. IB is a plan view of an alternate embodiment of the strut members and flexible linking elements including helical strut ring portions.
- Fig. 1C is a plan view of an alternate embodiment of the strut members and flexible linking elements including a single strut ring portion.
- Fig. ID is a plan view of an alternate embodiment of the strut members and flexible linking elements including multiple strut ring portions.
- Fig. IE is a schematic profile diagram of an alternative embodiment of the stent of the present invention in which strut members have a flared configuration.
- Fig. IF is a schematic profile diagram of an alternative embodiment of the stent of the present invention in which strut members have a larger diameter than the helical member.
- Fig. IG is a schematic profile diagram of an alternative embodiment of the stent of the present invention in which a helical member has a larger diameter than the stent members.
- Fig. IH is a schematic profile diagram of an alternative embodiment of the stent of the present invention in which strut members include barbs at either end thereof.
- Fig. II is a schematic profile diagram of an end view of the stent shown in Fig. IH.
- Fig. 2 A is a plan view of an alternate embodiment of the present invention having split helical elements interposed between strut members and connected to the strut members by flexible linking elements.
- Fig. 2B is a detailed view of Fig. 2A showing a portion of the split helical elements.
- Fig. 2C is a detailed view of an alternative embodiment of the helical element comprising a plurality of segments.
- Fig. 3 is a plan view of an alternate embodiment of the present invention having helical elements with thin sections interposed between strut members and connected to the strut members by flexible linking elements.
- Fig. 4 is a plan view of an alternate embodiment of the present invention comprising helical elements with thin diagonal sections with portions of the thin diagonal sections having a reduced width and curved flexible linking elements connecting the helical elements to the strut members.
- Fig. 5A is a plan view of an alternate embodiment of the present invention having a variable pitch of helical elements including curved sections having a reduced width and curved flexible linking elements connecting the helical elements to the strut members.
- Fig. 5B is a detail view of Fig. 5A showing the helical elements including curved sections having a reduced width
- Fig. 6A is a schematic diagram of a balloon expanding stent delivery system before inflation of the balloon with a stent on the balloon.
- Fig. 6B is a schematic diagram of a balloon expanding stent delivery system before inflation of the balloon without a stent on the balloon.
- Fig. 6C is a schematic diagram of a balloon expanding stent delivery system after partial inflation of the balloon without a stent on the balloon.
- Fig. 6D is an end view of Fig. 6C showing the rotation of the balloon expanding stent delivery system.
- Fig. 7A is an end cross section schematic representation of a self-expanding stent delivery system of the present invention prior to stent deployment.
- Fig. 7B is an end cross section schematic representation of a self-expanding stent delivery system of the present invention during stent deployment.
- Fig. IA is a plan view of a first embodiment of stent 10.
- the term plan view will be understood to be a 2 dimensional (2-D) view where the stent has been cut along the axis and laid out flat, such that the bottom edge could be wrapped around a cylinder and connected to the top edge.
- Stent 10 comprises strut members 12, helical elements 13 and flexible linking elements 14. In this , representation one of helical elements 13 has been shaded.
- Strut members 12 comprise one or more strut ring portions 15 and 16.
- Strut ring portions 15 and 16 comprise respectively a plurality of strut elements 17 and 18.
- strut elements 17 and 18 has been shaded.
- the plurality of strut elements 17 can be integral to one another.
- the plurality of strut elements 18 can be integral to one another.
- Connecting elements 19 connect strut elements 17 and 18 together at peaks 20 and 21.
- Connecting elements 19 can be rigid, flexible or of various predetermined lengths, for example, a helix configuration.
- Helical elements 13 are arranged in a side-by-side configuration in which each of helical elements 13 is helically wound about an axis of stent 10.
- Helical elements 13 are expandable radially upon deployment. In this embodiment, each helical element 13 makes more than one rotation about the surface of stent 10. However, they can make a partial rotation or one complete rotation.
- Strut member 12 generally provides an anchoring mechanism for stent 10 and comprises one or more strut ring portions 15 and 16 depending on the requirements of the stent. Strut ring portions 15 and 16 of strut member 12 provide radial structure and a mechanism for radial expansion of stent 10. In a preferred embodiment, strut member 12 is positioned at either end of stent 10. Strut member 12 being radially expandable upon deployment. Strut ring portions 15 and 16 can be formed of a variety of shapes and sizes to provide desired strength and stiffness upon expansion. For example, strut ring portions 15 and 16 can have a circumferential configuration in which strut ring portions 15 and 16 wrap around a circumference of stent 10 and each connects to itself.
- stent 10b includes strut ring portions 15b and 16b having a helical configuration in which strut ring portions 15b and 16b wrap in a spiral around the circumference of stent 10b and along the length of stent 10b, as shown in Fig. IB.
- Flexible linking element 14b can include a curved section for connecting helical element 13b to strut member 12b.
- Connecting elements 19b connect strut elements 17b and 18b together diagonally at peaks 20b and 21b. Accordingly, adjacent peaks 20b and 21b are offset diagonally from one another. Any number of strut ring portions 15 and 16 can be used in strut member 12.
- strut member 12c can comprise a single strut ring portion 15c, as shown in Fig. 1C, a pair of strut ring portions 15 and 16, as shown in Fig. IA, or multiple strut ring portions 15d connected together with connecting elements 19d, as shown in •Fig. ID.
- Connecting elements 19d connect adjacent strut ring portions 15d together diagonally at peaks 2Od and 2 Id in either diagonal direction Di and/or diagonal direction D 2 .
- Helical elements 13 can be connected with linking element 14 to each
- Linking element 14 can be flexible.
- helical elements 13 can connect to some of strut elements 17 as shown in Fig. IB.
- Fig. IB illustrates an embodiment in which every other strut member 17 is connected with linking element 14 to helical element 13. It will be appreciated that alternate combinations of connections of helical elements 13 to some of strut elements 17 can be used in accordance with the teachings of the present invention.
- strut members 12e can be flared to provide improved anchoring of stent 1Oe 5 as shown in Fig. IE.
- helical elements 13g have a larger diameter than strut member 12, as shown in Fig. IG.
- strut members 12f can have a bulged configuration in which strut member 12f has a larger diameter than helical elements 13 to provide improved anchoring, as shown in Fig. IF.
- Strut member 12 can have additional features to provide improved anchoring in the vessel.
- strut member 12g can include at least one barb 24 on distal end 22 and/or proximal end 23 of stent 1Og, as shown in Figs. IH and II.
- linking elements 14 connect strut members 12 to helical elements 13.
- Linking elements 14 allow the helix angle of helical elements 13 to change as the diameter of stent 10 increases during expansion.
- Linking elements 14 can be straight or curved.
- Diameter of stent 10 and Helix angle of helical elements 13 in an expanded and a crimped state are related by the following formula:
- De/Cos( ⁇ e) Dc/Cos( ⁇ c) (2) wherein De is the expanded stent diameter, ⁇ e is the expanded helix angle, Dc is the crimped diameter and ⁇ c is the crimped helix angle.
- the diameter of stent 10 gets larger and the helix angle of helical elements 13 decreases.
- the crimped diameter is limited by the helix angle, the width of helical elements 13 and number of helical elements 13.
- stent 10 comprised of helical elements 13 and linking elements 14 provides a high percentage of vessel covered by the stent, for example, such as a vessel near an aneurysm.
- the percentage of the portion of the vessel covered by the helical elements of the stent can be in the range of about 35% to about 90%.
- the percentage of the portion of the vessel covered by the helical elements of the stent is at least about 50%.
- Stent 10 provides an open area of about 10% to about 65%.
- Linking element 14 can have a length and shape to minimize the strain and optimize the expansion behavior of stent 10.
- Linking element 14 can have a thickening which varies along the length of linking element 14. This can include relatively straight and long links having a length of about 25% to about 50% of the circumference of stent 10.
- Linking element 14 can also comprise relatively straight and short links having a length in the range of about 10% to about 25% of the circumference of stent 10.
- linking elements 14 can comprise curved links as described below.
- Fig. 2A is a plan view of an alternate embodiment of stent 30.
- Stent 30 comprises helical element 33.
- Helical element 33 is split into two segments 34 and 35.
- Fig. 2B is a detailed view showing the two segments 34 and 35 comprising helical element 33.
- Splitting helical element 33 into a pair of segments improves crimping and expansion characteristics of stent 30, allowing helical element 33 to more easily change helix angle as the diameter of stent 30 expands from a crimped state to an expanded state.
- helical elements 33c can be split into a plurality of segments 34c, 35c, and 36c to provide additional improvement in the crimping and expansion characteristics, as shown in Fig. 2C.
- Fig. 3 is a plan view of an alternate embodiment of stent 40.
- Stent 40 comprises helical elements 43 having notches 44 at points along its length.
- Notches 44 create thin sections 45 of helical element 43.
- thin sections 45 can have a thickness of about 10% to about 80 % of the adjacent thicker portion 46 of helical element 43.
- Thin sections 45 created by notches 44 can act as hinge points and offers improved crimping and expansion characteristics allowing the helix angle of helical element 43 to more easily change helix angle as the diameter of stent 40 expands from a crimped state to an expanded state.
- notches 44 can be rectangular.
- thin sections 45 can be curved, circular, square, rectangular with fillets, and the like, and still provide improved crimping and expansion characteristics with different strain profiles.
- Fig. 4 shows an embodiment in which thin sections 45 are diagonal, for connecting adjacent portions 46a and 46b of helical element 43. Sections 45 have a thickness of about 10% to about 80% of portions 46a and 46b. Curved linking elements 51 connect helical elements 43 to strut member 12.
- Fig. 5A shows an embodiment in which thin sections 45 are curved and have a thickness of about 10% to about 80% adjacent portions 46.
- the pitch of helical element 43 changes along the length of stent 50 where the pitch is longer on left hand side 47 of stent 50 and shorter on right hand side 48 of stent 50. Varying the pitch in this manner changes the percent of vessel coverage along the length of the stent.
- stent 50 may be placed at an up-stream side of the aneurysm for effectively cutting off blood flow to the aneurysm, and left hand side 47 of stent 50 can be used in the down stream side for not entirely covering the aneurysm or vessel wall with stent material.
- Stent 50 also has curved flexible linking elements 52 connecting helical element 43 to strut member 12.
- Fig. 5B is a detailed view of thin section 45 of stent 50.
- the helical stents of the present invention may be placed within vessels using procedures well known in the art.
- the helical stents may be loaded into the proximal end of a catheter and advanced through the catheter and released at the desired site. Alternatively, the stent may be carried about the distal end of the catheter in a compressed state and released at the desired site.
- the stent may either be self- expanding or expanded by means such as an inflatable balloon segment of the catheter. After the stent(s) has been deposited at the desired intralumenal site, the catheter is withdrawn.
- the self expanding embodiment of the stent would not necessarily require additional expansion methods. However, the balloon expanding embodiment can use additional expansion methods. Expansion methods for a balloon expanding embodiment of the present invention are described below.
- a balloon expands the diameter of the stent and also rotates the helical elements such that the helix angle decreases, the pitch between helical elements shortens and the stent provides the desired vessel coverage of at least about 35% to about 90%, preferably about 50% of the portion of the vessel covered by the helical elements of the stent.
- Fig. 6A illustrates a balloon expanding delivery system 70 with a stent 40 mounted on the system.
- Fig. 6B illustrates balloon expanding delivery system 70 in a pre-inflated state, stent 40 has been omitted for clarity.
- Balloon 71 includes twists 72 which rotate in an opposite direction of helical elements 43.
- Twisted balloon 71 is placed within stent 40, as shown in Fig. 6A.
- Balloon 71 is inflated to an inflated state, as shown in Fig. 6C.
- a conventional self expanding stent delivery system utilizes an outer sheath to hold the stent in a crimped (radially compact) state and a pusher positioned at the proximal end of the stent which react the forces developed as the outer sheath is retracted during stent deployment.
- a conventional delivery system often has an inner tube which goes over a guide wire, also used during a typical procedure.
- Figs. 7A and 7B are cross sectional schematic representations illustrating self- expanding stent delivery system 90.
- Fig. 7 A shows stent 10 crimped and positioned within outer sheath 91.
- Pusher balloon 93 is positioned within stent 10 in a deflated state.
- Pusher balloon 93 is adjacent inner tube 94.
- Inner tube 94 can be a tube for a guide wire.
- Pusher balloon 93 is sized such that it can replace or augment the pusher positioned at the proximal end of the stent in a conventional delivery system as described above.
- pusher balloon 93 is inflated to a diameter about the same as the inside diameter of stent 10 in a crimped state.
- Pusher balloon 93 in its inflated state can distribute the reaction force developed during retraction of outer sheath 91 over the length of stent 10 instead of only at the proximal end. Accordingly, stent 10 does not significantly deform even though the axial stiffness of stent 10 is relatively low.
- fluid used to inflate pusher balloon 93 can be chilled to a temperature in the range of about -10° C to 10° C, thereby lowering the temperature of stent 10, reducing the outward force that stent 10 exerts on outer sheath 91, and lowering the reaction force developed to retract outer sheath 91.
- the stent of the present invention may be placed within body lumen such as neurovascular vessels of non-neurovascular vessels of any mammal species including humans, without damaging the lumenal wall.
- the stent can be placed within a lesion or an aneurysm for treating the aneurysm.
- the stent can be placed within a brain aneurysm for treating the brain aneurysm.
- the stent can be placed in a super femoral artery. Upon insertion into the vessel, the stent provides coverage of at least about 35% to about 90% of the portion of the vessel covered by the helical elements of the stent, preferably at least about 50% of the portion of the vessel covered by the helical elements of the stent.
- the stent of the present invention can be formed of any biocompatible material, such as stainless steel, titanium, gold, nickel-titanium (often referred to as shape-memory metal or "nitinol”) alloys, plastics and combinations thereof.
- biocompatible material such as stainless steel, titanium, gold, nickel-titanium (often referred to as shape-memory metal or "nitinol”) alloys, plastics and combinations thereof.
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- Heart & Thoracic Surgery (AREA)
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- Cardiology (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Physics & Mathematics (AREA)
- Vascular Medicine (AREA)
- Optics & Photonics (AREA)
- Animal Behavior & Ethology (AREA)
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- Prostheses (AREA)
Abstract
La présente invention concerne un stent fournissant un pourcentage élevé de couverture de vaisseau, de préférence au moins environ 50 % de la partie du vaisseau recouverte par les éléments hélicoïdaux du stent. Le stent comprend des éléments hélicoïdaux interposés entre des éléments d'étai, les éléments hélicoïdaux étant connectés aux éléments d'étai par des éléments de liaison. La partie du stent ayant des éléments hélicoïdaux fournit un pourcentage élevé de zone recouverte par exemple, dans une zone d'anévrisme. Les éléments de liaison fournissent une partie du mécanisme qui permet à une couverture de vaisseau d'être maintenue lorsque le stent est déployé d'un état serti à un état élargi, permettant aux éléments hélicoïdaux de changer leur angle d'hélice (l'angle suivant lequel les éléments hélicoïdaux progressent autour de la périphérie et le long de la longueur du stent) et par conséquent le pas des éléments hélicoïdaux à mesure que le stent est élargi.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US11/497,069 | 2006-08-01 | ||
US11/497,069 US8956400B2 (en) | 2005-10-14 | 2006-08-01 | Helical stent |
Publications (2)
Publication Number | Publication Date |
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WO2008016626A2 true WO2008016626A2 (fr) | 2008-02-07 |
WO2008016626A3 WO2008016626A3 (fr) | 2008-12-04 |
Family
ID=38997686
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/US2007/017152 WO2008016626A2 (fr) | 2006-08-01 | 2007-08-01 | Stent hélicoïdal |
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US (1) | US8956400B2 (fr) |
WO (1) | WO2008016626A2 (fr) |
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Cited By (10)
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US10123804B2 (en) | 2011-05-11 | 2018-11-13 | Covidien Lp | Vascular remodeling device |
US11045204B2 (en) | 2011-05-11 | 2021-06-29 | Covidien Lp | Vascular remodeling device |
EP2773286A1 (fr) * | 2011-11-04 | 2014-09-10 | Reverse Medical Corporation | Dispositif de pontage pour anévrisme en saillie et procédé d'utilisation associé |
EP2773286A4 (fr) * | 2011-11-04 | 2014-11-05 | Reverse Medical Corp | Dispositif de pontage pour anévrisme en saillie et procédé d'utilisation associé |
US9072620B2 (en) | 2011-11-04 | 2015-07-07 | Covidien Lp | Protuberant aneurysm bridging device deployment method |
US9241815B2 (en) | 2011-11-04 | 2016-01-26 | Covidien Lp | Protuberant aneurysm bridging device and method of use |
EP3095415A1 (fr) * | 2011-11-04 | 2016-11-23 | Covidien LP | Dispositif de pontage d'anévrisme saillant et procédé d'utilisation |
US9763815B2 (en) | 2011-11-04 | 2017-09-19 | Covidien Lp | Protuberant aneurysm bridging device deployment method |
US10624772B2 (en) | 2011-11-04 | 2020-04-21 | Covidien Lp | Protuberant aneurysm bridging device deployment method |
US11406519B2 (en) | 2011-11-04 | 2022-08-09 | Covidien Lp | Protuberant aneurysm bridging device deployment method |
Also Published As
Publication number | Publication date |
---|---|
US20070129786A1 (en) | 2007-06-07 |
WO2008016626A3 (fr) | 2008-12-04 |
US8956400B2 (en) | 2015-02-17 |
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